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rs35849660

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs35849660(A;A)
Make rs35849660(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5248400
GeneHBG1
is asnp
is mentioned by
dbSNPrs35849660
ebirs35849660
HLIrs35849660
Exacrs35849660
Varsomers35849660
Maprs35849660
PheGenIrs35849660
hapmaprs35849660
1000 genomesrs35849660
hgdprs35849660
ensemblrs35849660
gopubmedrs35849660
geneviewrs35849660
scholarrs35849660
googlers35849660
pharmgkbrs35849660
gwascentralrs35849660
openSNPrs35849660
23andMers35849660
23andMe allrs35849660
SNP Nexus

SNPshotrs35849660
SNPdbers35849660
MSV3drs35849660
GWAS Ctlgrs35849660
Max Magnitude0
OMIM142200
Desc
Variant0029
Relatedalso


ClinVar
Risk rs35849660(A;A)
Alt rs35849660(A;A)
Reference rs35849660(G;G)
Significance Other
Disease HEMOGLOBIN F (JIANGSU)
Variation info
Gene HBG1
CLNDBN HEMOGLOBIN F (JIANGSU)
Reversed 1
HGVS NC_000011.9:g.5269630C>T
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016176.1,



[PMID 1703137] Hb F-Jiangsu, the first gamma chain variant with a valine----methionine substitution: alpha 2A gamma 2 134(H12)Val----Met.